HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39305Erstellt: 23. Oktober 2026
Triethylamine → 2-(Pyridin-2-ylmethoxy)-isoindole-1.3-dione
https://huagongshe.com/de/reaction/39305
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | Picolyl chloride hydrochloride | HCID 23392 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(Pyridin-2-ylmethoxy)-isoindole-1.3-dione | HCID 12213945 | 46% |
Reaktionsschritte
2-Chloromethylpyridine hydrochloride (514 mg, 3.13 mmol), N-hydroxyphthalimide (515 mg, 3.18 mmol), and triethylamine (1.3 mL, 9.3 mmol) were mixed in acetonitrile (5 mL) and stirred at 80° C. for 2.5 hours. The reaction mixture was diluted with ethyl acetate and washed sequentially with 1N NaOH(aq), water, and brine. The organic phase was dried over MgSO4, filtered, and concentrated. The residue was recrystallized from ethyl acetate and hexanes to provide N-(pyridine-2-ylmethoxy)phthalimide (364 mg, 1.44 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524764B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-a0c6c07c91f64f5fb80b8604da9ff8f9 |
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| Quellennotiz | uspto-grants-2013_09 |
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